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Satellite lesions versus intrahepatic metastasis in multifocal intrahepatic cholangiocarcinoma: Prognostic impact and genomic profiling

  • Tao Wei
  • , Zhi Jie Ma
  • , Shouliang Guo
  • , Matthew Weiss
  • , Irinel Popescu
  • , Hugo P. Marques
  • , Luca Aldrighetti
  • , Shishir K. Maithel
  • , Carlo Pulitano
  • , Todd W. Bauer
  • , Feng Shen
  • , George A. Poultsides
  • , Oliver Soubrane
  • , Guillaume Martel
  • , Bas Groot Koerkamp
  • , Itaru Endo
  • , Tingbo Liang
  • , Yi Lyu
  • , Timothy M. Pawlik
  • , Xu Feng Zhang
  • The First Affiliated Hospital of Xi’an Jiaotong University
  • Zhejiang University
  • Johns Hopkins University
  • Fundeni Clinical Institute
  • Hospital Curry Cabral
  • Ospedale San Raffaele
  • Emory University
  • The University of Sydney
  • University of Virginia
  • Eastern Hepatobiliary Surgery Hospital
  • Stanford University
  • Department of Hepatobiliopancreatic Surgery
  • University of Ottawa
  • Erasmus University Rotterdam
  • Yokohama City University
  • Ohio State University

科研成果: 期刊稿件文章同行评审

7 引用 (Scopus)

摘要

Background and Aims: – Multifocal intrahepatic cholangiocarcinoma (ICC) is typically categorized as satellite lesions (SL) or intrahepatic metastasis (IM). Clinical staging and prognostic significance of multifocal ICC are topics of debate. Approach and Results: – ICC patients with solitary or multifocal tumors undergoing curative-intent surgical resection were identified from an international multi-institutional database. SL and IM were classified according to distribution patterns. Among 1064 patients included in the cohort, 358 had multifocal tumors that were defined as IM (n=95) or SL (n=263). Isolated AJCC stage II of multifocal ICC disease was associated with shorter overall (OS) (median: 26.1 vs. 60.0 mo, p<0.001) and disease-free survival (DFS) (median DFS: 9.8 vs. 25.0 mo, p<0.01) than solitary tumors within stage II, yet had a comparable prognosis as stage III disease. Patients with IM or SL had comparable OS and DFS (both p>0.1), regardless of tumor number status. Genomic profiling demonstrated a highly concordant mutational landscape of IM and SL in 24 multifocal ICC patients. Phylogenetic and evolutionary trajectory analysis supported that multifocal lesions with different distribution patterns were of the same origin, derived from the corresponding primary tumors. In addition, single-nucleus RNA sequencing revealed that both IM and SL harbored increased levels of copy number variations compared with the primary lesion, indicative of malignant progression. Conclusions: – Multifocal ICC should be categorized as AJCC stage III disease regardless of IM and SL patterns. Both SL and IM are clonally derived from the primary ICC tumor and represent metastatic progression with poor long-term survival.

源语言英语
期刊Hepatology
Publish Ahead of Print
DOI
出版状态已出版 - 1 1月 2025
已对外发布

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